Beschreibung
InhaltsangabeWhat Would Thomas Henry Huxley Have Made of Prion Diseases? Rosalind M. Ridley Prion Protein as Copper-Binding Protein at the Synapse Hans A. Kretzschmar, Tobias Tings, Axel Madlung, Armin Giese, and Jochen Herms A Function for the Prion Protein? David R. Brown and Ian M. Jones Prion Protein Peptide: Agents of Death for Neurons David R. Brown Characterization of Bovine Spongiform Encephalopathy and Scrapie Strains/Isolates by Immunochemical Analysis of PrPSc Martin H. Groschup, Frauke Junghans, Martin Eiden, and Thorsten Kuczius Differential Targeting of Neurons by Prion Strains Stephen J. DeArmond Transgenic Studies of Prion Diseases Glenn C. Telling Prions: From Neurografts to Neuroinvasion Markus Glatzel, Sebastian Brandner, Michael A. Klein, and Adriano Aguzzi Cellular and Transgenic Models of Familial Prion Diseases David A. Harris, Roberto Chiesa, Antonio Migheli, Pedro Piccardo, and Bernardino Ghetti Central Nervous System Inflammation and Prion Disease Pathogenesis Samar Betmouni and V. Hugh Perry The Electroneuropathology of Prion Disease J. Richard Greene Transmissible Spongiform Encephalopathy Neurobiology and Ultrastructure Suggests Extracellular PrPSc Conversion Consistent with Classical Amyloidosis Martin Jeffrey and Jan R. Fraser Conformation as Therapeutic Target in the Prionoses and Other Neurodegenerative Conditions Thomas Wisniewski, Einar M. Sigurdsson, Pierre Aucouturier, and Blas Frangione Prions of Yeast: From Cytoplasmic Genes to Heritable Amyloidosis Reed B. Wickner, Herman K. Edskes, Kimberly L. Taylor, Marie-Lise Maddelein, Hiromitsu Moriyama, and B. Tibor Roberts
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